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rs864622273

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864622273(A;A)
Make rs864622273(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position62813412
GeneEGR2
is asnp
is mentioned by
dbSNPrs864622273
ebirs864622273
HLIrs864622273
Exacrs864622273
Varsomers864622273
Maprs864622273
PheGenIrs864622273
hapmaprs864622273
1000 genomesrs864622273
hgdprs864622273
ensemblrs864622273
gopubmedrs864622273
geneviewrs864622273
scholarrs864622273
googlers864622273
pharmgkbrs864622273
gwascentralrs864622273
openSNPrs864622273
23andMers864622273
23andMe allrs864622273
SNP Nexus

SNPshotrs864622273
SNPdbers864622273
MSV3drs864622273
GWAS Ctlgrs864622273
Max Magnitude0
ClinVar
Risk rs864622273(A;A)
Alt rs864622273(A;A)
Reference rs864622273(G;G)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene EGR2
CLNDBN Charcot-Marie-Tooth disease, type I
Reversed 1
HGVS NC_000010.10:g.64573172C>T
CLNSRC
CLNACC RCV000206846.1,